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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421076Generated: October 26, 2026

Hydrochloric Acid → 3-Hydroxy-5,5-dimethyl-4-[4-(methylsulfonyl)phenyl]-2(5H)-furanone

https://huagongshe.com/reaction/1421076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetoxyacetyl chlorideHCID 26297—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant2-Hydroxy-2-methyl-1-(4-(methylsulfonyl)phenyl)propan-1-oneHCID 15428514—
SolventPyridineHCID 1049—
SolventAcetonitrileHCID 6342—
Product3-Hydroxy-5,5-dimethyl-4-[4-(methylsulfonyl)phenyl]-2(5H)-furanoneHCID 1554220462%

Reaction Steps

To a 0° C. solution of the alcohol of Example 1, Step 3 (29.5 g, 122 mmol) in CH3CN (350 mL) were added pyridine (25 mL) and acetoxyacetyl chloride (25 g, 183 mmol). After a period of 7 h at r.t., DBU (31 mL) was added to the reaction mixture. After a period of 1 h at 80° C., a second portion of DBU (35 mL) was added. The reaction mixture was kept at 80° C. for 18 h. The reaction mixture was allowed to cool to r.t. The mixture was poured onto ice-water (2.5 L) containing 100 mL of concentrated HCl. The brown solid was collected and dissolved in hot acetonitrile and was filtered through a plug of silica. The solvent was evaporated and the resultant solid was swished in EtOAc to give the title compound (21.2 g, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06071954
Source datasetuspto-grants-2000_06
ORD IDord-27809ef581f64dc6a1db8811621e182c
Source noteuspto-grants-2000_06